66907-73-1 Usage
Chemical class
Tetrazoles are a class of organic compounds that contain a tetrazolyl ring, which is a five-membered ring with four nitrogen atoms and one carbon atom.
Structure
1-(biphenyl-2-yl)-1H-tetrazol-5-amine consists of a tetrazole ring with an attached biphenyl group, and an amine group at the 5th position of the tetrazole ring.
Pharmacological activities
Tetrazoles are known for their diverse pharmacological activities, which include anti-inflammatory, anti-cancer, and anti-bacterial properties.
Potential applications
1-(biphenyl-2-yl)-1H-tetrazol-5-amine may have potential applications in pharmaceutical research and drug development due to its unique structure and functional groups.
Building block
1-(biphenyl-2-yl)-1H-tetrazol-5-amine is a valuable building block for the synthesis of novel bioactive molecules.
Research implications
Further research on 1-(biphenyl-2-yl)-1H-tetrazol-5-amine could lead to the discovery of new drugs with improved therapeutic properties.
Molecular weight
The molecular weight of 1-(biphenyl-2-yl)-1H-tetrazol-5-amine is approximately 251.29 g/mol.
Solubility
The solubility of 1-(biphenyl-2-yl)-1H-tetrazol-5-amine may vary depending on the solvent used, but it is generally soluble in polar solvents like water and methanol.
Stability
Tetrazoles are generally stable compounds, but the stability of 1-(biphenyl-2-yl)-1H-tetrazol-5-amine may be influenced by factors such as temperature, light exposure, and the presence of other reactive substances.
Check Digit Verification of cas no
The CAS Registry Mumber 66907-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,0 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66907-73:
(7*6)+(6*6)+(5*9)+(4*0)+(3*7)+(2*7)+(1*3)=161
161 % 10 = 1
So 66907-73-1 is a valid CAS Registry Number.
66907-73-1Relevant academic research and scientific papers
Selective Gold-Catalysed Synthesis of Cyanamides and 1-Substituted 1H-Tetrazol-5-Amines from Isocyanides
?koch, Karel,Císa?ová, Ivana,?těpni?ka, Petr
supporting information, p. 13788 - 13791 (2018/09/14)
The newly discovered gold-catalysed reaction of isocyanides with hydrazoic acid generated in situ from trimethylsilyl azide and methanol (or, alternatively, from NaN3/AcOH) produces either cyanamides or 1-substituted 1H-tetrazol-5-amines, depending on the amount of available HN3. The reaction proceeds selectively and in generally high yields of either product, thus providing a particularly convenient access to a wide range of substituted 1H-tetrazol-5-amines that are rather difficult to access otherwise.
